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GTDC1,糖基转移酶样1抗体

GTDC1,糖基转移酶样1抗体

商家询价

产品名称: GTDC1,糖基转移酶样1抗体

英文名称: Anti-GTDC1 antibody

产品编号: HZ-8582R

产品价格: null

产品产地: 中国/美国

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: WB,ELISA,IHC-P,IHC-F,IF

上海沪震实业有限公司
  • 联系人 : 鲍丽雯
  • 地址 : 上海市闵行区闵北路88弄1-30号第22幢AQ136室
  • 邮编 : 200612
  • 所在区域 : 上海
  • 电话 : 139****0749
  • 传真 : 021-60345367
  • 邮箱 : www.shzbio.net

GTDC1,糖基转移酶样1抗体

产品编号HZ-8582R
英文名称GTDC1
中文名称糖基转移酶样1抗体
别 名Glycosyltransferase like 1; Glycosyltransferase like domain containing 1; Glycosyltransferase like domain containing protein 1; Mannosyltransferase candidate; GTDC1_HUMAN.
说 明 书0.1ml 0.2ml
研究领域细胞生物 免疫学 发育生物学
抗体来源Rabbit
克隆类型Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Pig, Horse, Rabbit, Zebrafish,
GTDC1,糖基转移酶样1抗体产品应用WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量53kDa
性 状Lyophilized or Liquid
浓 度1mg/1ml
免 疫 原KLH conjugated synthetic peptide derived from human GTDC1
亚 型IgG
纯化方法affinity purified by Protein A
储 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件Store at -20 癈 for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20癈. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 癈.
GTDC1,糖基转移酶样1抗体PubMedPubMed
产品介绍background:
Glycosyltransferases that mediate the regio- and stereoselective transfer of sugars, such as the fucosyltransferases, determine cell surface-carbohydrate profiles, which is an essential interface for biological recognition processes. GTDC1 (Glycosyltransferase-like domain-containing protein 1), also known as Mat-Xa, is a 458 amino acid protein belonging to the glycosyltransferase 1 family. GTDC1 is ubiquitously expressed, with highest levels found in peripheral blood leukocytes, spleen, lung and testis.An extremely rare recessive genetic disorder, Alstr鰉 syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.

Tissue Specificity:
biquitous. Expressed at high levels in the lung, spleen, testis and peripheral blood leukocytes.

Similarity:
Belongs to the glycosyltransferase group 1 family. Glycosyltransferase 4 subfamily.

Database links:
UniProtKB/Swiss-Prot: Q4AE62.1

GTDC1,糖基转移酶样1抗体Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.