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ABCD1 antibody

产品编号:2098-1

产品描述:ABCD1 antibody

反应种属:Mouse

实验方法:WB

标记:

规格:100ul

供应商:Epitomics

价格(RMB):2100.00

订购:订购

说明书:

ABCD1 antibody

Cat.#: 2098-1

Rabbit Monoclonal Antibody

Clone ID: EP1363Y
Swiss Prot: O88430
Mol Weight: 8kDa
Size: 100ul

Description

Chemokines are a large family of small secreted proteins that regulate migration of white blood cells. Based on the arrangement of the first two of the four conserved cysteine residues, chemokines are classified into four subfamilies, CXC, CC, C and recently identified CX3C (1). The CC chemokines, in which the first 2 cysteines are adjacent, usually act on monocytes, T lymphocytes, and, in some cases, eosinophils, basophils, or mast cells. The CC subfamily proteins are 70 to 100 amino acids long, have 25 to 75% identity with each other, and include novel member of the CC chemokine subfamily, designated ABCD1 (SCYA22). The SCYA22 protein shares 28 to 34% identity with other CC chemokines and contains the characteristic 4-cysteine motif and 9 other highly conserved residues (2). The activated T cell-attracting CC chemokine CCL22 is expressed by stimulated B cells and mature dendritic cells (DC). Both identical and distinct proteins contribute to expression of CCL22 in DC and B cells (3).

Recommended Applications

WB

Applications and Recommended Dilution Factors

WB: 1:250 - 500

Species Reactivity

Mouse


Products Data


A. Western blot analysis on 5 ng mouse MDC recombinant protein using anti-ABCD-1 RabMAb (cat. # 2098-1), dilution 1:500.
  
  

Specificity

A synthetic peptide corresponding to residues near the C-terminus of mouse ABCD-1 was used as an immunogen.

Storage Buffer & Conditions

50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA.

Alternative Names

Ccl22, Abcd1, Scya22, C-C motif chemokine 22, Small-inducible cytokine A22;CC chemokine ABCD-1;Activated B and dendritic cell-derived

Description References

1. Nomiyama H, et al. Cytogenetics and Cell Genetics 81:10-11, 1998.
2. Godiska R, et al. J Exp Med 185(9):1595-604, 1997.
3. Ghadially H, et al. J Immunol 174(9):5620-9, 2005.